LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Question on neuro lyme treatment?

 - UBBFriend: Email this page to someone!    
Author Topic: Question on neuro lyme treatment?
bv
LymeNet Contributor
Member # 9578

Icon 1 posted      Profile for bv     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have neuro lyme (burning skin, muscle twitches, muscle jerks, floaters, flashing lights etc)> Been on doxy & a cyst buster for 8 months=doc switched me to ceftin in place of doxy. Doc does not think iv treatment necessary.

Here is the question. Everything i read says neuro lyme needs iv or intra musular rocephin to be cured. I am concerned I am missing a window of opportunity to treat the spirocheetes.

Please tell me if you have had iv treatment & was it helpful. How often (daily?). Thank you for your response.

Posts: 213 | From ohio | Registered: Jul 2006  |  IP: Logged | Report this post to a Moderator
savebabe
Frequent Contributor (1K+ posts)
Member # 9847

Icon 1 posted      Profile for savebabe     Send New Private Message       Edit/Delete Post   Reply With Quote 
Both IM bicillin LA and IV doxy were very successful treatments for me.

The key is to combat the co-infections before treating the lyme with IV.

Posts: 1603 | From ny | Registered: Aug 2006  |  IP: Logged | Report this post to a Moderator
Bill ATL
Member
Member # 7817

Icon 1 posted      Profile for Bill ATL     Send New Private Message       Edit/Delete Post   Reply With Quote 
BV...how many different combos of Oral Abx have you tried? Did they help? Miminal reaction?

What is status/severity of your current health?

My LLMD would base his oral vs IV decision based mostly on current health state.

If in bad shape physically and bad cognitive, then IV may be warranted...but if you could function somewhat normal day to day, then he may want to try oral abx. Mine changed them after a periods of "no response" until we found one that made an impact...which happen to be Zithro and Mepron (with Artemisinin).

Most Drs base their Oral vs IV decisions based on your whole health picture....shying away from invasive (picc line or IV) procedures.

just my $0.02

--------------------
Bill

**Question everything...it may save your life!!!**

Posts: 80 | From ATLantic Seaboard | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
davidx
LymeNet Contributor
Member # 8326

Icon 1 posted      Profile for davidx     Send New Private Message       Edit/Delete Post   Reply With Quote 
This is a great question and one that I wrestle with myself. I dont think there is any hard and fast rule. I think people respond differently.

With that said, after a certain amount of time on orals, if your symptoms arent getting better then it is probably worth trying IV. This is sort of the conclusion that I am coming to. With that said, IV does not guarantee you'll get better...but hopefully it will help!

-Davud

--------------------
Same nightmare, different day!

Posts: 401 | From East Coast | Registered: Nov 2005  |  IP: Logged | Report this post to a Moderator
Visual Afterimage Man
LymeNet Contributor
Member # 10435

Icon 1 posted      Profile for Visual Afterimage Man     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm neuro lyme infected. 90% of my complaints are neuro related. I have been on orals for 5 months now.

Doxy and Omnicef. I have seen some improvement. I did ask my LLMD about IV and he said that it's not a necessary step for me at this point in treatment. People tend to herx harder on IV and can find themselves unable to work. He has seen people respond to orals and become cured (or remission whatever you want to call it) but just a a slower rate.

So here's how I see it.

IV = Bad Herx's, knocks you on your butt for months. Expensive and health insurance will only allow so many treatments before the bill becomes yours.

Orals = Less severe herx. Longer duration of treatment, but doesn't knock people on their butts as badly. Insurance doesn't complain as much because it's much cheaper.

If you don't respond to 12 months of Orals, then I would definatly ask the Dr to TRY the IV.

As for a window of opportunity.. I'm not sure that there is such a thing. If you are on abx then you are getting some benefit. I don't belive you have a certain amount of time to kill the Lyme before you become uncurable... Try to hang in there and don't put so much pressure on yourself.

--------------------
26 months of treatment. And counting.......

Posts: 298 | From Northeast Kansas | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.